Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2248839 1.000 0.040 7 38301625 upstream gene variant C/T snv 0.85 1
rs2331599 1.000 0.040 14 22268778 intron variant T/C snv 0.39 1
rs2392545 1.000 0.040 7 38303396 upstream gene variant G/A snv 0.33 1
rs2392546 1.000 0.040 7 38303484 upstream gene variant G/A snv 0.14 1
rs2534567 1.000 0.040 7 38319355 upstream gene variant C/A snv 0.18 1
rs2534568 1.000 0.040 7 38320039 upstream gene variant G/A snv 0.18 1
rs2534575 1.000 0.040 7 38331873 upstream gene variant T/A;C snv 1
rs2534578 1.000 0.040 7 38333930 upstream gene variant T/A;C snv 1
rs2734222 1.000 0.040 7 142780026 upstream gene variant T/A;C snv 1
rs2734224 1.000 0.040 7 142780878 upstream gene variant A/C;G snv 1
rs2735179 1.000 0.040 7 38325004 upstream gene variant T/C snv 0.29 1
rs2736964 1.000 0.040 7 38305168 upstream gene variant T/C snv 0.51 1
rs2736969 1.000 0.040 7 38304355 upstream gene variant A/C snv 0.11 1
rs2736973 1.000 0.040 7 38302014 upstream gene variant A/C snv 0.86 1
rs3811272 1.000 0.040 14 22273851 intron variant C/T snv 0.29 1
rs3853524 1.000 0.040 1 143665797 intergenic variant C/A;T snv 1
rs4726572 1.000 0.040 7 142717016 upstream gene variant C/A snv 7.9E-02 1
rs4982590 1.000 0.040 14 22250515 intron variant G/A snv 0.14 1
rs6462829 1.000 0.040 7 38292616 upstream gene variant C/T snv 0.15 1
rs6464528 1.000 0.040 7 142717058 upstream gene variant G/A snv 3.9E-02 1
rs6572261 1.000 0.040 14 22103621 upstream gene variant C/T snv 8.3E-02 1
rs6572331 1.000 0.040 14 22246958 intron variant G/A snv 0.15 1
rs6572349 1.000 0.040 14 22268365 intron variant C/T snv 0.22 1
rs6572351 1.000 0.040 14 22268415 intron variant C/T snv 0.47 1
rs6673776 1.000 0.040 1 143566021 intron variant T/A;C snv 3.3E-02 1